Institute for Diabetes and Cancer, Helmholtz Munich, Neuherberg, Germany.
Joint Heidelberg-IDC Translational Diabetes Program, Inner Medicine 1, Heidelberg University Hospital, Germany.
Mol Oncol. 2024 Sep;18(9):2070-2086. doi: 10.1002/1878-0261.13590. Epub 2024 Feb 27.
Cancer cachexia (Ccx) is a complex metabolic condition characterized by pronounced muscle and fat wasting, systemic inflammation, weakness and fatigue. Up to 30% of cancer patients succumb directly to Ccx, yet therapies that effectively address this perturbed metabolic state are rare. In recent decades, several characteristics of Ccx have been established in mice and humans, of which we here highlight adipose tissue dysfunction, muscle wasting and systemic inflammation, as they are directly linked to biomarker discovery. To counteract cachexia pathogenesis as early as possible and mitigate its detrimental impact on anti-cancer treatments, identification and validation of clinically endorsed biomarkers assume paramount importance. Ageing was recently shown to affect both the validity of Ccx biomarkers and Ccx development, but the underlying mechanisms are still unknown. Thus, unravelling the intricate interplay between ageing and Ccx can help to counteract Ccx pathogenesis and tailor diagnostic and treatment strategies to individual needs.
癌症恶病质(Ccx)是一种复杂的代谢紊乱,其特征是明显的肌肉和脂肪消耗、全身炎症、虚弱和疲劳。多达 30%的癌症患者直接死于 Ccx,但有效的治疗方法却很少。近几十年来,在小鼠和人类中已经确定了 Ccx 的几个特征,我们在这里重点强调脂肪组织功能障碍、肌肉消耗和全身炎症,因为它们与生物标志物的发现直接相关。为了尽早对抗恶病质的发病机制,并减轻其对癌症治疗的不利影响,鉴定和验证临床认可的生物标志物至关重要。最近的研究表明,衰老会影响 Ccx 生物标志物的有效性和 Ccx 的发展,但潜在的机制尚不清楚。因此,揭示衰老与 Ccx 之间的复杂相互作用有助于对抗 Ccx 的发病机制,并针对个体需求调整诊断和治疗策略。